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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Ureteral catheter holder FDA UDI
Device Name
SECUREMENT,TUBE,F/FOLEY CATH,STERILE FDA UDI
Model / Reference
DYND7600FCL FDA UDI
Description
SECUREMENT,TUBE,F/FOLEY CATH,STERILE FDA UDI

Identifiers

Catalog Number
DYND7600FCL FDA UDI
Primary DI / UDI-DI
10884389245682 FDA UDI
FDA Product Code
EYJ FDA UDI
GMDN Term
Ureteral catheter holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ureteral catheter holder

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral catheter holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 9d9e1bc7-f586-4e1d-ab5c-502bcd3da519 36 fields · synced May 30, 2026